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胆道闭锁

Biliary atresia.

作者信息

Howard E R, Tan K C

机构信息

King's College Hospital, London.

出版信息

Br J Hosp Med. 1989 Feb;41(2):123-4, 128-30.

PMID:2653529
Abstract

Biliary atresia remains a serious and devastating surgical condition of early childhood. Despite portoenterostomy almost half of these children remain jaundiced and suffer repeated attacks of bacterial cholangitis or variceal haemorrhage. Recently liver transplantation offers fresh hope for these children.

摘要

胆道闭锁仍然是幼儿期一种严重且具有破坏性的外科病症。尽管进行了肝门肠吻合术,但这些儿童中仍有近一半持续黄疸,并反复遭受细菌性胆管炎发作或静脉曲张出血。最近,肝移植为这些儿童带来了新的希望。

相似文献

1
Biliary atresia.胆道闭锁
Br J Hosp Med. 1989 Feb;41(2):123-4, 128-30.
2
Surgical experience in children with biliary atresia treated with portoenterostomy.经门静脉肠吻合术治疗儿童胆道闭锁的手术经验。
Curr Surg. 2005 Jul-Aug;62(4):439-43. doi: 10.1016/j.cursur.2004.11.022.
3
[Hepatic portoenterostomy and primary liver transplantation in the treatment of biliary atresia].[肝门空肠吻合术及原位肝移植治疗胆道闭锁]
Lijec Vjesn. 2001 Nov-Dec;123(11-12):317-22.
4
The extent of biliary proliferation in liver biopsies from patients with biliary atresia at portoenterostomy is associated with the postoperative prognosis.在施行肝门空肠吻合术的胆道闭锁患者的肝脏活检中,胆管增生的程度与术后预后相关。
J Pediatr Surg. 2009 Apr;44(4):695-701. doi: 10.1016/j.jpedsurg.2008.09.013.
5
Biliary atresia--surgical management and treatment options as they relate to outcome.胆道闭锁——与预后相关的手术管理及治疗选择
Liver Transpl Surg. 1998 Sep;4(5 Suppl 1):S24-33.
6
Pregnancy in biliary atresia after kasai operation complicated by portal hypertension.肝门空肠吻合术后合并门静脉高压的胆道闭锁患者的妊娠情况。
J Med Assoc Thai. 2006 Nov;89(11):1961-4.
7
Jaundice clearance and cholangitis in the first year following portoenterostomy for biliary atresia.先天性胆道闭锁行肝门空肠吻合术后第一年的黄疸清除情况及胆管炎
Med J Malaysia. 2002 Mar;57(1):92-6.
8
[Late complications after successful Kasai's operation for biliary atresia].[先天性胆道闭锁行成功的葛西手术后的晚期并发症]
Nihon Geka Gakkai Zasshi. 1989 Sep;90(9):1348-52.
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Hepatolithiasis after hepatic portoenterostomy for biliary atresia.先天性胆管闭锁肝门空肠吻合术后肝内胆管结石
J Pediatr Surg. 2006 Apr;41(4):808-11. doi: 10.1016/j.jpedsurg.2005.12.036.
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Kasai portoenterostomy--new insights from hepatic morphology.肝门空肠吻合术——肝脏形态学的新见解
J Pediatr Surg. 2005 Feb;40(2):322-6. doi: 10.1016/j.jpedsurg.2004.10.018.

引用本文的文献

1
Expression of programmed death-1 and its ligands in the liver of biliary atresia.程序性死亡受体 1 及其配体在胆道闭锁肝脏中的表达。
World J Pediatr. 2017 Dec;13(6):604-610. doi: 10.1007/s12519-017-0018-5. Epub 2017 Mar 22.